Clinical Research Coordinator

Clinical Research CoordinatorFlourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction. Shift: Full time, Monday-Friday, 8:30 - 5 PM (flexibility needed depending on patient schedules) Location: Walnut Creek, CA Compensation: $24-$33 per hour RESPONSIBILITIESExecute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.Obtain informed consent per federal regs, GCP, and IRB requirements.Ethically recruit qualified subjects to meet enrollment timelines.Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.Schedule and conduct visits per protocol timelines.Protect confidentiality per HIPAA and all confidentiality agreements.Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.Represent Flourish professionally in all interactions.Additional duties as assigned by management.